Gene-specific Copy Number Variation Probe-BRWD1
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| Catalog: |
CNVFP-BRWD1-01529 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (BRWD1). The product usually consists of a combination of reagents, which consists of a probe with a selected dye color and a hybridization reagent. We provide CNV FISH Probes with a variety of dye color combinations to meet various challenges. Probe products not only provide some classic color combinations but also provide customized probe services. |
| Application: |
BRWD1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to BRWD1 genes. This product achieves the purpose of detection by hybridizing with the BRWD1 gene. Due to this design method, our probe products can detect the amplification and deletion of target genes on chromosomes through FISH. |
| Category: |
Copy Number Variation |
| Probe Kits Volume (µL): |
40 μL |
| Quantity: |
20 Tests |
| Hybridization Solution (µL): |
200 μL |
| Turnaround Time: |
7-10 Business Days |
| Shipping Time: |
1-2 Day Expedited Shipping |
| Storage Conditions: |
Store at -20℃ and avoid light; |
| Shipping Conditions: |
-20℃ |
Gene Details
| Gene Name |
Bromodomain And WD Repeat Domain Containing 1 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD) residues which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes including cell cycle progression, signal transduction, apoptosis, and gene regulation. This protein contains 2 bromodomains and multiple WD repeats. This gene is located within the Down syndrome region-2 on chromosome 21. Alternative splicing of this gene generates multiple transcript variants encoding distinct isoforms. In mouse, this gene encodes a nuclear protein that has a polyglutamine-containing region that functions as a transcriptional activation domain which may regulate chromatin remodelling and associates with a component of the SWI/SNF chromatin remodelling complex.[provided by RefSeq, Jun 2011] |
| Gene Symbol |
BRWD1 |
| Location |
21q22.2 |
| Chromosome |
Chromosome21 |
| Coordinates |
This gene maps to 40557403-40685712 in GRCh37 coordinates. |
| Species |
Human |
Dye Colors:
OR
RE
GO
GR
AQ
Order Sheet
| Number |
Dye Color |
Order Name |
Absorbance Maximum |
Emission Maximum |
Add to Cart |
| 1 |
OR
|
CNVFP-BRWD1-01529-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-BRWD1-01529-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-BRWD1-01529-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-BRWD1-01529-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-BRWD1-01529-AQ |
467nm |
418nm |
|
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